WormBase Tree Display for DO_term: DOID:0070269
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DOID:0070269 | Name | congenital disorder of glycosylation type IIq | |||
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Status | Valid | ||||
Definition | A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the COG2 gene on chromosome 1q42.2. | ||||
Synonym | Exact | CDG IIq | |||
CDG2Q | |||||
CDGIIdq | |||||
COG2-CDG | |||||
COG2-related congenital disorder of glycosylation | |||||
Parent | Is_a | DOID:0050571 | |||
DOID:0050737 | |||||
DB_info | Database | OMIM | disease | 617395 | |
Attribute_of | Gene_by_orthology | WBGene00000585 |